KE501: Kemi 1 – Fundamental Chemistry (10 ECTS)

STADS: 10005901

Level
Bachelor course

Teaching period
The course is offered in the autumn semester.
1st and 2nd quarter.

Teacher responsible
Email: mip@ifk.sdu.dk
Email: pon@ifk.sdu.dk

Timetable
Group Type Day Time Classroom Weeks Comment
Common I Monday 13-14 U55 35-41, 45-49
Common I Wednesday 13-14 U55 35-41, 45-48
Common I Thursday 12-13 U55 35-41, 45-49
S1 TE Tuesday 08-10 U49b 35-40, 45-51
S1 TE Tuesday 16-18 U49c 51
S1 TE Thursday 10-12 U144 44
S1 TE Thursday 08-10 U27a 49
S1 TE Thursday 12-14 U49b 50
S2 TE Tuesday 10-12 U49c 51
S2 TE Wednesday 08-10 U49b 35-40, 45-48,50-51
S2 TE Wednesday 12-14 U144 49
S2 TE Friday 10-12 U144 44
S2 TE Friday 14-16 U49b 49-50
S3 TE Monday 14-16 U49b 49-51
S3 TE Wednesday 16-18 U49d 51
S3 TE Thursday 08-10 U49b 35-40, 45-50
S3 TE Thursday 12-14 U144 44
S4 TE Monday 16-18 U103 51
S4 TE Tuesday 14-16 U49c 49-51
S4 TE Thursday 10-12 U37 39
S4 TE Friday 08-10 U49b 35-38,40, 45-50
S4 TE Friday 14-16 U144 44
S5 TE Tuesday 14-16 U49b 35-40, 45-51
S5 TE Wednesday 14-16 U49c 49-51
S5 TE Thursday 13-15 U142 44
S6 TE Monday 16-18 U89a 51
S6 TE Tuesday 10-12 U49 39
S6 TE Wednesday 14-16 U49b 35-38,40, 45-51
S6 TE Thursday 14-16 U49b 49-50
S6 TE Friday 12-14 U7 44
S8 TE Monday 08-10 U9 51
S8 TE Tuesday 08-10 U28 50
S8 TE Tuesday 16-18 U49e 51
S8 TE Wednesday 12-14 U49 49
S8 TE Thursday 10-12 U49b 35-41, 49-50
S8 TE Thursday 10-12 U26 45-48
S10 TE Monday 14-16 U17 47
S10 TE Monday 14-16 U69a 51
S10 TE Tuesday 12-14 U17 49
S10 TE Wednesday 10-12 U66 50
S10 TE Wednesday 10-12 U49e 51
S10 TE Friday 08-10 U93 35-38
S10 TE Friday 10-12 U49e 39
S10 TE Friday 10-12 U145 40
S10 TE Friday 10-12 U49 44
S10 TE Friday 10-12 U17 45,49-50
S10 TE Friday 10-12 U145 47
S10 TE Friday 10-12 U26 48
S11 TE Tuesday 08-10 U130 35
S11 TE Tuesday 08-10 U74 36-40,45-48,50
S11 TE Tuesday 08-10 U103 51
S11 TE Wednesday 14-16 U132 49-51
S11 TE Thursday 14-16 U17 49
S11 TE Friday 12-14 U144 44
S12 TE Monday 08-10 U68 36-40,46-51
S12 TE Tuesday 10-12 U49b 51
S12 TE Thursday 12-14 U9 44
S12 TE Friday 14-16 U49b 35, 45,49-50
S13 TE Monday 14-16 U49b 36-40
S13 TE Monday 14-16 U144 45-51
S13 TE Wednesday 08-10 U103 35,50-51
S13 TE Wednesday 10-12 U57 49
S13 TE Thursday 14-16 U144 44
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Revison of timetable:
: S10 flyttet uge 47 og 49 efter ønske.
: Undervisning d. 23 og 24 dec. flyttet.
: S10 fredag uge 40 rykket fra 08-10 til 10-12 efter ønske.
: S8 eksaminatorietime flyttet fra mandag morgen uge 49 til onsdag kl. 12-14 uge 49.
: E-timer flyttet fra uge 41 til uge 44 (Gælder dog ikke S8)
: S10 fredag 2.kvartal rykket til kl. 10-12. Se skema for lokaler!!
: S4 og S10 flyttet fredag uge 39.
: S2e flyttet onsdag uge 49 fra kl. 08-10 til kl. 12-14.
: Skema opdateret med tilrettede hold.

Prerequisites:
None

Academic preconditions:
None.

Course introduction
The aim of the course is to provide the students with knowledge of chemistry at such a level that the acquired knowledge can form the background of advanced studies within chemistry and support related disciplines, e.g. biology, biochemistry, biotechnology, bioinformatics, biomedicine, pharmaceutical sciences, physics and chemical engineering.

Expected learning outcome
For the examination, the students are expected to be able to:
- describe the connection between quantum numbers and orbitals
- explain the significance of different types of chemical bonding and recognize the concept of hybridisation
- relate knowledge on chemical bonding, orbitals and hybridization to problems in general chemistry
- draw Lewis-structures for simple molecules and ions and argue for their geometry using the VSEPR-model
- recognize the concept of resonance in the context of simple inorganic molecules and ions
- employ Le Chatelier’s principle on chemical equilibria and perform calculations on equilibrium mixtures from equilibrium constants
- explain the concept of intermolecular interactions
- determine concentrations from titrations and equilibrium constants and relate pH-calculations to the titration curves for acid/base titrations
- recognize reaction types of zero, first and second order, employ integrated reaction rate equations, Arrhenius' equation and recognize catalysis and molecularity
- determine reaction order, half lives and activation energies from experimental data
- recognize and employ the concepts of enthalpy, entropy, heat capacity, free energy and solubility constant in simple calculations
- recognize and employ the fundamental concepts of Galvanic and electrolytic cells, Faraday’s law and Nernst’s equation
- perform calculations of concentrations, potentials and equilibrium constants
- read and draw organic chemical structures and formula
- recognize the basic structures and the functional groups and to assess the relevance of these for the properties of concrete compounds including polarity, reactivity in aqueous solutions and the possibility for intermolecular bonds.
- explain the most common reactions for different organic classes of compounds based on basic structures and functional groups including saturated and unsaturated carbon hydrides, aromatic compounds, halogen compounds, alcohols, ethers, amines and carbonyl compounds.
- employ the nomenclature for simple organic molecules and recognize the most common trivial names
- employ the basic concepts for stereochemistry and isomerism as well as the concepts configuration and conformation
- employ simple mechanisms in the explanation of the most common reactions
- explain the most important aspects of nucleophilic substitution, electrophilic addition and elimination.
- explain the most important aspects of electrophilic aromatic substitution and employ the concept of resonance in accordance to organic molecules.
- explain the use of condensation, hydrolysis, oxidation and reduction.
- describe and suggest simple organic syntheses from a judgment of basic structures and functional groups as well as the reactivity of these
- interpret simple 13C NMR-spectra
- relate chemical reactivity to practical experiment

Subject overview
  • Atomic structure related to the construction of the periodic table
  • Concepts concerning the chemical bonding, includingCovalent and non-covalent bonding
  • Molecular structure, including Aliphatic and aromatic hydrocarbons and alkyl halides, Functional groups, stereochemistry and nomenclature
  • Chemical equilibrium, including Acids and bases, buffers and ampholytes Solubility product and heterogeneous equilibria
  • Thermodynamics, including The first law of thermodynamics, energy and enthalpy, The second law of thermodynamics, entropy and free energy, Electrochemistry
  • Reaction kinetics
  • Organic chemical reactions, including The concept of resonance and reaction mechanisms, Alcohols, phenols and ethers, aldehydes and ketones, Carboxylic acids, carboxylic acid derivatives and amines, Keto-enol tautomerism, Elimination, Nucleophilic substitution, Electrophilic aromatic substitution
Literature
  • Blackman et al.: Chemistry, Wiley 2008. 7000


Syllabus
See syllabus.

Website
This course uses e-learn (blackboard).

Prerequisites for participating in the exam
None

Assessment and marking:
a) Delivery of acceptable answers to at least 10 out of 12 exercises. Pass/fail, internal examination by the teacher. Gives 1 ECTS.

b) A 4 hour written exam after the 2nd quarter with all aids allowed. The exam incorporates elements from KE501A and KE501S. External marking and grade according to the 7-points scale.

Re-examination after 4th quarter.

Expected working hours
The teaching method is based on three phase model.

Forelæsninger (36 t), eksaminatorier og opgaveregning (34 t).
Educational activities

Language
This course is taught in Danish.

Remarks
The 10 ECTS includes following two 1 ECTS elements: KE501A and KE501S

Course enrollment
See deadline of enrolment.

Tuition fees for single courses
See fees for single courses.